Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01673776
Other study ID # FEMO
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2012
Est. completion date October 15, 2016

Study information

Verified date August 2018
Source Technische Universität München
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is designed to compare the outcome of patients with proximal femoral fractures with different perioperative regimes: a group with a multimodal intervention and a control group.


Description:

Femoral neck fractures constitute both a social and economic challenge. The one year mortality of affected patients amounts to 33%, wherein cardio-vascular complications are the major contributor. It is an objective of the present study to investigate whether a multi-modal perioperative intervention can improve the outcome of these patients.

We plan to carry out a prospective randomized controlled clinical study. Patients with an age above 60 years and proximal femoral fractures (femoral neck fractures or pertrochanteric femoral fractures) are to be included. These are divided into two groups, K and M. General anaesthesia is applied to both groups. In group K a commonly used therapy will be applied whereas in group M an intesified perioperative care will be carried out. The objectives are to provide sufficient analgesia, normotonia and normothermia. Hence, a femoral catheter is applied for pain therapy already preoperatively. Moreover, the pulmonal situation is improved by means of oxygen as needed. The cardiovascular situation is evaluated and optimized by means of extended hemodynamic monitoring both pre- and postoperatively. If needed, the nutrition of the patients is supplemented with highly caloric drinks.

A primary common endpoint is the appearance of postoperative complications. These include cardiovascular, cerebrovascular, pulmonal, renal and surgical complications. Secondary endpoints are mortality, duration of the stay at the hospital and intensive care duration. It is the objective of the study to reduce the probability for at least one postoperative complication from 50% to 25% (α=0,05 and 1-β=0,80). To this end 132 patients would have to be included in the study.

All participants are to be contacted by phone one year after the surgery and their health situation is to be determined.


Recruitment information / eligibility

Status Completed
Enrollment 132
Est. completion date October 15, 2016
Est. primary completion date October 2016
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria:

- proximal femoral fracture (femoral neck fracture/ pertrochanteric femoral fracture)

- Age = 60 years

- written informed consent

Exclusion Criteria:

- pathological fracture

- multiple trauma

- fracture during a hospital stay due to a different disease

Study Design


Intervention

Device:
PulsioFlex® Monitoring
goal directed therapy according to PulsioFlex® Monitoring- measurements femoral catheter extended perioperative monitoring nutritional supplementation, (if necessary)

Locations

Country Name City State
Germany Klinik für Anaesthesiologie, Klinikum rechts der Isar der Technischen Universität München Munic Bavaria

Sponsors (1)

Lead Sponsor Collaborator
Technische Universität München

Country where clinical trial is conducted

Germany, 

References & Publications (2)

Hamilton MA, Cecconi M, Rhodes A. A systematic review and meta-analysis on the use of preemptive hemodynamic intervention to improve postoperative outcomes in moderate and high-risk surgical patients. Anesth Analg. 2011 Jun;112(6):1392-402. doi: 10.1213/ANE.0b013e3181eeaae5. Epub 2010 Oct 21. Review. — View Citation

Pedersen SJ, Borgbjerg FM, Schousboe B, Pedersen BD, Jørgensen HL, Duus BR, Lauritzen JB; Hip Fracture Group of Bispebjerg Hospital. A comprehensive hip fracture program reduces complication rates and mortality. J Am Geriatr Soc. 2008 Oct;56(10):1831-8. doi: 10.1111/j.1532-5415.2008.01945.x. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative complications postoperative complications: cardiovascular, cerebrovascular, pulmonal, renal and surgical complications The participants will be followed for the duration of hospital stay, an expected average of 14 days
Secondary mortality 1 year
Secondary duration of the stay at the hospital 1 year
Secondary intensive care duration 1 year
See also
  Status Clinical Trial Phase
Active, not recruiting NCT00859378 - Cemented vs Non-cemented Semiendoprosthesis in the Treatment of Proximal Femoral Fractures N/A
Active, not recruiting NCT06351943 - Proximal Femur Image Database Validation
Completed NCT03768622 - Proximal Femoral Fractures - Patient Population, Risk Factors, Surgical Performance and Outcome
Completed NCT03975868 - Risk Factors for Cut-out After Internal Fixation of Trochanteric Fractures in Elderly Subjects.